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Clinical Trial Summary

The aim of this study is to compare exercise capacity in Chronic Obstructive Pulmonary Disease (COPD) patients before and after an 8 week pulmonary rehabilitation program.

Patients will be randomised in two groups, one arm will received oxygen through High Flow Nasal Cannula (HFNC) and the other group by The Venturi Mask (VM)


Clinical Trial Description

Design: randomized, single blind, controlled trial.

The main goal of this study is to compare the exercise tolerance in COPD patients after an 8 week pulmonary rehabilitation program using High Flow Nasal Cannula or The Venturi Mask. The exercise tolerance will be measured in seconds in a Constant Load Treadmill Test (CTLT). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02973945
Study type Interventional
Source Hospital Italiano de Buenos Aires
Contact Nicolas NR Roux, PT-RT
Phone +5411 4959 0200
Email nicolas.roux@hospitalitaliano.org.ar
Status Recruiting
Phase N/A
Start date July 1, 2017
Completion date May 2019

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